Infusion Device

ABSTRACT

The disclosures made herein relate to an infusion device specifically adapted for syringe injections. In one embodiment of the disclosures made herein, an infusion device comprises a body including an accessible surface having a single inlet port therein, an engagement surface having a single outlet port therein, a medication delivery channel extending between the single inlet port and the single outlet port, and an identification feature on the accessible surface of the body adjacent to the single inlet port. The single inlet port of the medication delivery channel is tapered thereby forming a funnel-shaped entry into the medication delivery channel. A cannula is coupled to the body at the single outlet port and is adapted for receiving medication from the single outlet port and transmitting the medication therethrough.

CROSS-REFERENCE TO RELATED APPLICATION

This is a continuation of co-pending application Ser. No. 10/188,591,filed Jul. 2, 2002, which is incorporated by reference withoutdisclaimer.

FIELD OF THE DISCLOSURE

The disclosures herein relate generally to infusion devices and method,and more particularly to a subcutaneous infusion device specificallyadapted for receiving therapeutic substances injected with a syringe.

BACKGROUND

Presently, the delivery options available to insulin dependent diabeticsfor insulin delivery include direct injections with a syringe,continuous-delivery with an insulin pump and injections with ajet-spray. Each one of these insulin delivery options has advantages,disadvantages and limitations with respect to factors such asconvenience, cost, effort, safety, reliability and pain. Accordingly,selection of an acceptable delivery option by a diabetic will depend onthe advantages of a selected insulin delivery option as well as thediabetic's ability and willingness to tolerate the limitations anddisadvantages of the selected insulin delivery option.

One of the most reliable methods of insulin delivery that a diabetic canchoose is direct injection with a syringe (i.e., an injection needlepierces the skin). Direct injection with a syringe offers precisemeasurement of insulin and the security of manual delivery. However,direct injection with a syringe sometimes necessitates multipleinjections during the course of a day. For example, a Type-1 diabeticgenerally needs a dosage of insulin either immediately before or after ameal.

For many diabetics, their aversion to needles precludes them from everbeing able to bring themselves to direct injection with a syringe. Forother diabetics, multiple direct injections per day and bruises at theinjection site become too much to tolerate. Regardless of the particularreason or reasons, there are a large number of diabetics who cannotbring themselves to inject their insulin directly with a needle or wholose their ability to tolerate direct injections with a syringe. Thesediabetics often under-medicate themselves, endangering their physicalhealth and mental well being.

Many diabetics who choose not to subject themselves to multiple directinjections with a syringe, because they have a fear of needles and/orbecause they bruise easily, look to other options besides directinjections with a syringe. For those who simply have a fear of needles,but are able to tolerate the pain and bruises associated with injectionneedles, jet spray injection is an option. Jet spray injection deliversa fine stream of insulin through the skin under extreme high pressure.Although a needle is not used, jet spray injection exhibits a similarlevel of pain and bruising associated with its use as do directinjections with a syringe.

The insulin pump has become the most popular option for diabetics whocannot face multiple daily direct injections with a syringe. With theinsulin pump, a diabetic receives a continuous dosage of insulin from apump apparatus via an infusion device mounted on their body. Insulin issupplied (e.g., pumped) from the insulin pump through a tube to theinfusion device. Infusion devices generally include a cannula mountingin a subcutaneous manner within the flesh of the diabetic. The infusiondevice includes a channel that transmits insulin from an inlet port tothe cannula for being delivered to the subcutaneous tissue layer of thediabetic.

Mounting of the infusion device generally involves the use of aninsertion needle. Most conventional infusion devices have an insertionneedle that extends through a body of the device and through thecannula. During mounting of such a conventional infusion device, theinsertion needle serves to pierce the skin and to support the cannula,as most cannulas are made from a soft and/or flexible material.Accordingly, the diabetic still must deal with a needle piecing theirskin. However, because the infusion device may remain in place for anextended period of time (e.g., typically up to 3 days or more), thediabetic need only deal with one injection type needle over 3 or moredays, rather than multiple times per day. This extended period of timebetween needle insertions is what makes the pump tolerable for manydiabetics who have an aversion to being pierced with injection needles.

The advantages of the insulin pump do not come without a number ofsignificant disadvantages. One disadvantage is that the precisemeasurement of insulin and the security of manual delivery associatedwith direct injections with a syringe are largely turned over to theinsulin pump. Situations such as the pump malfunctioning, degradation ofthe insulin within the pump reservoir (e.g., due to heat), bubbles inthe reservoir/supply tube of the pump (e.g., due to agitation) andinherent limitations of an electromechanical device often result in thepump delivering an incorrect dosage of insulin. As the pump is acontinuous delivery device, the diabetic may not know that they arereceiving an incorrect dosage of insulin until a lengthy period of timehas passed, resulting in dangerous blood-sugar levels. Anotherdisadvantage is that the insulin pump, which is about the size of atypical pager, must be worn essentially 24 hours per day. Finding aninconspicuous yet convenient place to wear the pump can be difficult.Still another disadvantage is the cost of the insulin pump—about $8000for the pump, plus disposable supplies. Though insurance plans generallycover insulin pumps, the considerable price of the pump adverselyaffects insurance premiums. Furthermore, under certain insurancepolicies, the insured party may still have the responsibility of payingfor at least a portion of the pump.

Therefore, a device and method for enabling a frequently administeredmedication to be injected with a syringe in a manner that overcomeslimitations associated with conventional medication delivery devices andmethods.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view depicting a single cannula infusion devicein accordance with a first embodiment of the disclosures made herein.

FIG. 2 is a cross-sectional view taken at the line 2-2 in FIG. 1.

FIG. 3 is cross-sectional view depicting a single cannula infusiondevice in accordance with a second embodiment of the disclosures madeherein, wherein the infusion device includes a self-sealing membermounted on an accessible surface a body of the infusion device andwherein the a single outlet port is offset from an engagement surface ofthe body.

FIG. 4 is a cross-sectional view depicting a single cannula infusiondevice in accordance with a third embodiment of the disclosures madeherein, wherein a self-sealing member is attached adjacent to anengagement surface of a body of the infusion device.

FIG. 5 is a cross-sectional view depicting a single cannula infusiondevice in accordance with a fourth embodiment of the disclosures madeherein, wherein a first self-sealing member is attached adjacent to anaccessible surface of a body of the infusion device and a secondself-sealing member is attached adjacent to an engagement surface of thebody of the infusion device.

FIG. 6 is a cross-sectional view depicting a single cannula infusiondevice in accordance with a fifth embodiment of the disclosures madeherein, wherein a needle stop is attached within a medication deliverychannel of a body of the infusion device.

FIG. 7 is a cross-sectional view depicting a multi-cannula infusiondevice in accordance with a sixth embodiment of the disclosures madeherein, wherein a plurality of self-sealing members are mounted adjacentto respective medication delivery channels and wherein a first cannulais a different length than a second cannula.

FIG. 8 is a cross-sectional view depicting a multi-cannula infusiondevice in accordance with a seventh embodiment of the disclosures madeherein, wherein a single self-sealing member is attached to anaccessible surface of a body of the infusion device thereby forming aseptum for each one of a plurality of medication delivery channels.

DETAILED DESCRIPTION OF THE FIGURES

The disclosures made herein relate to various aspects of an infusiondevice specifically adapted for receiving an injection from a syringe.As discussed in greater detail below, such an infusion device isbeneficial to any patient (e.g., human patients or animal patients) thatrequires receiving medication via some type of direct injection on adaily basis. Insulin-dependent diabetics are an example of a patientthat requires receiving medication via some type of trans-dermalmedication delivery on a daily basis. In fact, a typicalinsulin-dependent diabetic require multiple trans-dermal injections ofinsulin daily.

An infusion device in accordance with embodiments of the disclosuresmade herein is mountable on a patient with the cannula extending into orthrough subcutaneous tissue of a patient. Once the infusion device ismounted on the patient, the patient may use a syringe and injectionneedle for receiving an injection of one or more medications via theinfusion device. The patient is spared having their skin pierced by theinjection needle. After an initial skin piercing by an insertion needleof the infusion device, all injections are facilitated via the injectionneedle being engaged with the infusion device rather than through theskin of the patient. The patient would only be subjected to piecing ofthe skin by a needle when replacing an existing mounted infusion devicewith a new infusion device. Depending on factors associated with thepatient, the medication, the specific construction of the infusiondevice, it is contemplated herein that the infusion device would onlyneed to be replaced every three days or more.

An infusion device in accordance with an embodiment of the disclosuresmade herein permits patients who might not otherwise choose directinjection with a syringe due to as their primary mode of medicationdelivery for any number of reasons (e.g., an aversion to needles, anintolerance to bruises at an injection site, etc) to now do so. Throughthe use of such an infusion device, a patient may enjoy the precisemeasurement of a medication and/or the security of manual deliveryafforded by direct injection with a syringe. It should be noted thatdirect injection is one of the most reliable methods of self-deliverythat a patient can choose. This reliability is due at least in part tothis precise measurement of the medication and the security of manualdelivery. In essence, a patient has direct control over when, where andhow much medication they are receiving. Accordingly, infusion devices inaccordance with embodiments of the disclosures made herein aid inenabling patients to properly medicate themselves, thus maintainingtheir health and mental well being.

Another advantage of an infusion device in accordance with an embodimentof the disclosures made herein is the ability to easily conceal theinfusion device, without hindering access to it. The size and profile ofthe infusion device permits it to be worn inconspicuously under clothingat various portions of the patient's body. While not directly related toa patient's physiological health, being able to readily conceal theinfusion device under nearly any garment goes a long way to enhancingthe mental well-being of human patients.

Still another advantage of an infusion device in accordance with anembodiment of the disclosures made herein is its cost. Its cost is afraction of other delivery devices intended to reduce anxiety and/ordiscomfort associated with direct injections with a syringe. Itsrelatively low cost will be of benefit to patients, doctors andinsurance companies.

Turning now to the drawing figures, FIGS. 1 and 2 depicts a infusiondevice 10 in accordance with a first embodiment of the disclosures madeherein. The infusion device 10 includes a body 12, a cannula 14, aself-sealing member 16 and an adhesive laminate member 17. The body 12includes an accessible surface 18 having a single inlet port 20 therein,an engagement surface 22 having a single outlet port 24 therein and amedication delivery channel 26 extending between the single inlet port20 and the single outlet port 24. The infusion device 10 represents anembodiment of a single cannula infusion device in accordance with thedisclosures made herein.

The cannula 14 is coupled to the body 12 at the single outlet port 24.The cannula 14 is adapted for receiving medication from the singleoutlet port 24 and transmitting the medication through a channel 28 ofthe cannula. The cannula 14 and the medication delivery channel 26 havean essentially straight, common longitudinal axis. The essentiallystraight, common longitudinal axis extends generally perpendicular tothe engagement surface 22 of the body 12. Although the engagementsurface 22 is depicted as being essentially planar, it is contemplatedand disclosed herein that the engagement surface may have a profileother than essentially planar. Furthermore, it is contemplated hereinthat in other embodiments of infusion devices as disclosed herein, themedication delivery channel 26 and the associated cannula 14 do not havean essentially straight, common longitudinal axis.

The self-sealing member 16 is mounted at least partially within themedication delivery channel 26 with an exposed surface of theself-sealing member 16 being essentially contiguous with the accessiblesurface 18 of the body 12. The self-sealing member 16 forms a septumextending across the medication delivery channel 26. The septum limitscontaminants entering the medication delivery channel 26 and limits theback-flow of medication from the medication delivery channel 26 throughthe single inlet port 20.

The adhesive laminate member 17 is mounted on the engagement surface 22of the body 12. The adhesive laminate member 17 includes an adhesivelayer disposed between a substrate layer and a release liner layer. Thesubstrate layer provides structural integrity for the adhesive layer andis attached to the body 12. The release liner is removable from theadhesive layer for engaging the adhesive layer to be bonded to a skinsurface of the patient during mounting of the infusion device 10,thereby securing the infusion device 10 to a patient's body. It iscontemplated that the substrate layer may be omitted or integral withthe body 12 in other embodiments (not shown) of the disclosures madeherein.

The medication delivery channel 26 includes a tapered portion 30adjacent to the accessible surface 18 of the body 12. The taperedportion 30 of the medication delivery channel 26 forms a funnel-shapedentry into the medication delivery channel 26. The tapered portion 30 isintended to aid a patient in engaging an injection needle 32 of asyringe 34 in a relatively quick and convenient manner by providing aninsertion area for the needle 32 that is suitably larger than a crosssectional area of the injection needle 32.

The tapered portion 30 of the medication delivery channel 26 is taperedin a manner such that the single inlet port 20 has a minor diametricaldimension at least about two times greater than a minor diametricaldimension of the medication delivery channel 26. A nominal diametricaldimension of an essentially non-tapered portion of the medicationdelivery channel (e.g., adjacent to the single outlet port 24) is anexample of the minor diametrical dimension of the medication deliverychannel 26. Examples of port and channel cross-sectional profilesinclude round, rectangular, triangular, elliptical and other knownprofiles. In one embodiment of the single inlet port 20 and themedication delivery channel 26, the single inlet port 20 and themedication delivery channel 26 each have a substantially circularcross-sectional profile and the single inlet port 26 is essentiallycircular. In such an embodiment, the opening (i.e., a circular shapedopening) has a diameter at least about two times greater than a minordiameter of the medication delivery channel.

The body 12 further includes an identification feature 36 on theaccessible surface 18 encompassing the single inlet port 20. Theidentification feature 36 is intended to aid in identifying the singleinlet port 20. The identification feature 36 is raised with respect tothe accessible surface 18 of the body 12.

It is contemplated herein that identification features in accordancewith embodiments of the disclosures made herein may be at leastpartially raised with respect to an accessible surface of a respectivebody, may be at least partially recessed with respect to an accessiblesurface of a respective body or a combination of both raised andrecessed with respect to an accessible surface of a respective body. Itis also contemplated herein that identification features in accordancewith embodiments of the disclosures made herein may be a different colorthan a respective body and/or self-sealing material. It is yet furthercontemplated herein that identification features in accordance withembodiments of the disclosures made herein may be any one of a pluralityof shapes (e.g., round, rectangular, triangular, elliptical, etc.). Itis still further contemplated herein that identification features inaccordance with embodiments of the disclosures made herein may be asymbol (e.g., a Braille symbol) or a shape positioned adjacent to arespective inlet port, but not encompassing that port.

FIG. 3 depicts an infusion device 100 in accordance with a secondembodiment of the disclosures made herein. The infusion device 100 issimilar in structure to the infusion device 10 depicted in FIGS. 1 and2. Structural elements and features of the infusion device 100 and theinfusion device 10 (depicted in FIGS. 1 and 2) are similarly denoted.For example, the body of the infusion device 100 is denoted as 112,whereas the body of the infusion device 10 is denoted as 12. Suchsimilar elements and features are denoted for clarity in FIG. 3, but maynot be discussed in specific detail in reference to FIG. 3.

The infusion device 100 includes a body 112, a self-sealing member 116mounted on an accessible surface 118 of the body 112 and a single outletport 124 that is offset from an engagement surface 122 of the body 112.The self-sealing member 116 forms a septum extending across themedication delivery channel 126. The septum limits contaminants enteringthe medication delivery channel 126 and limits the back-flow ofmedication from the medication delivery channel 126 through the singleinlet port 120. Although the self-sealing member 116 is depicted ascovering only a portion of the accessible surface 118 of the body 112,it is contemplated and disclosed herein that the self-sealing member 116may cover essentially the entire accessible surface 118 of the body 112.

The self-sealing member 116 includes an integral identification feature136. The identification feature 136 encompasses the single inlet port120 of the medication delivery channel 126. The identification feature136 is intended to aid in identifying the medication delivery channel126. The identification feature 136 is raised with respect to an exposedsurface of the self-sealing member 116. It is contemplated herein thatidentification features in accordance with embodiments of thedisclosures made herein may be at least partially raised with respect tothe exposed surface of a respective self-sealing member, may be at leastpartially recessed with respect to an exposed surface of a respectiveself-sealing member or a combination of both raised and recessed withrespect to an exposed surface of a respective self-sealing member.

FIG. 4 depicts an infusion device 200 in accordance with a thirdembodiment of the disclosures made herein. The infusion device 200 issimilar in structure to the infusion device 10 depicted in FIGS. 1 and2. Structural elements and features of the infusion device 200 and theinfusion device 10 (depicted in FIGS. 1 and 2) are similarly denoted.For example, the body of the infusion device 200 is denoted as 212,whereas the body of the infusion device 10 is denoted as 12. Suchsimilar elements and features are denoted in FIG. 4, but may not bediscussed in specific detail in reference to FIG. 4.

The infusion device 200 includes a body 212 and a self-sealing member216. The self-sealing member 216 is mounted on the body 212 adjacent toan engagement surface 222 of the body 212 and at least partially withinthe medication delivery channel 226. The self-sealing member 216 forms aseptum extending across the medication delivery channel 226 adjacent toa single outlet port 224 of the body 212. The septum limits contaminantsentering the channel 228 of the cannula 214 and limits the back-flow ofmedication from the cannula through the single outlet port 224.

FIG. 5 depicts an infusion device 300 in accordance with a fourthembodiment of the disclosures made herein. The infusion device 300 issimilar in structure to the infusion device 10 depicted in FIGS. 1 and2. Structural elements and features of the infusion device 300 and theinfusion device 10 (depicted in FIGS. 1 and 2) are similarly denoted.For example, the body of the infusion device 300 is denoted as 312,whereas the body of the infusion device 10 is denoted as 12. Suchsimilar elements and features are denoted in FIG. 5, but may not bediscussed in specific detail in reference to FIG. 5.

The infusion device 300 includes a body 312, a first self-sealing member316 mounted on the body 312 adjacent to an accessible surface 318 of thebody 312 and a second self-sealing member 319 mounted on the body 312adjacent to an engagement surface 322 of the body 312. The firstself-sealing member 316 forms a septum extending across the medicationdelivery channel 326 adjacent to a single inlet port 320 of the body 312(i.e., the first septum). The second self-sealing member 319 forms aseptum extending across the medication delivery channel 326 adjacent toa single outlet port 324 of the body 312 (i.e., the second septum). Thefirst septum limits contaminants entering the medication deliverychannel 326 and limits the back-flow of medication from the medicationdelivery channel 326 through the single inlet port 320. The secondseptum limits the back-flow of medication from the medication deliverychannel 326 through the single inlet port 320. An advantage of thesecond septum is that the volume of the medication delivery channel istaken out of the dosage amount (i.e., medication does not sit stagnantin the medication delivery channel) when the injection needle isproperly inserted through both the first and the second septum prior todelivering the medication.

FIG. 6 depicts an infusion device 400 in accordance with a fifthembodiment of the disclosures made herein. The infusion device 400 issimilar in structure to the infusion device 10 depicted in FIGS. 1 and2. Structural elements and features of the infusion device 400 and theinfusion device 10 (depicted in FIGS. 1 and 2) are similarly denoted.For example, the body of the infusion device 400 is denoted as 412,whereas the body of the infusion device 10 is denoted as 12. Suchsimilar elements and features are denoted in FIG. 6, but may not bediscussed in specific detail in reference to FIG. 6.

The infusion device 400 includes a body 412 having an accessible surface418 with a single inlet port 420 therein, an engagement surface 422having a single outlet port 424 therein and a medication deliverychannel 426 extending between the single inlet port 420 and the singleoutlet port 424. A needle stop 438 is positioned adjacent to the singleoutlet port 424 of the medication delivery channel 426. The needle stopmay be a discrete component attached to the body 412 or may beintegrally formed with the body 412. The needle stop 438 limits thedepth to which an injection needle can be inserted into the medicationdelivery channel 430.

One advantage of limiting the insertion depth of an insertion needle isthat the needle is prevented from damaging (e.g., piercing) the cannula414. Even when a needle that is too long relative to an intended useneedle is used with the infusion device 400, the needle stop 438precludes the needle from piercing through the cannula 414 or piercinginto the patient's flesh adjacent to the cannula 414. Another advantageof limiting the insertion depth of an insertion needle is that theoverall height of the body 412 can be reduced. Because the insertiondepth of an injection needle is physically limited by the needle stop438, the overall length of the medication delivery channel 426 (i.e.,the distance between the single inlet port 420 and the single outletport 424) no longer serves to limit over insertion of an injectionneedle. Accordingly, the overall height of the body 412 can be reducedwith respect to a body without a needle stop, without concern for overinsertion of an injection needle.

FIG. 7 depicts an infusion device 500 in accordance with a sixthembodiment of the disclosures made herein. The infusion device 500includes a body 512, a plurality of cannulas 514, a plurality ofself-sealing members 516 and an adhesive laminate member 517. The body512 includes an accessible surface 518 having a plurality of singleinlet ports 520 therein, an engagement surface 522 having a plurality ofsingle outlet ports 524 therein and a discrete medication deliverychannel 526 extending between a respective one of the single inlet ports520 and a respective one of the single outlet ports 524. Each discretemedication channel 526 is associated with only one of the single inletports 520 and only one of the single outlet ports 524.

Each discrete medication delivery channel 526 is spaced apart from anadjacent discrete medication delivery channel 526 by a prescribeddistance. Factors such as the type(s) of medication and the frequency ofinjections delivered via the infusion device 500 influence theprescribed distance. The term discrete in reference to medicationdelivery channel refers to each medication delivery channel beingseparate from each other medication delivery channel. The infusiondevice 500 represents an embodiment of a multi-cannula infusion devicein accordance with the disclosures made herein.

Each one of the cannulas 514 is coupled to the body 512 at a respectiveone of the single outlet ports 524. Each one of the cannulas 514 isadapted for receiving medication from the respective one of the singleoutlet ports for transmitting the medication through a channel 528 ofthe corresponding one of the cannulas 514. A first one of the cannulas514 is a different length than a second one of the cannulas. It iscontemplated that in other embodiments of multi-cannula infusion devicesin accordance with the disclosures made herein, all of the cannulas areessentially the same length.

Each medication delivery channel 526 and the associated one of saidcannulas 514 have a common, essentially straight longitudinal axis. Thecommon, essentially straight longitudinal axis extends generallyperpendicular to the engagement surface 522 of the body 512. Althoughthe engagement surface 522 is depicted as being essentially planar, itis contemplated and disclosed herein that the engagement surface 522 mayhave a profile other than essentially planar. Furthermore, it iscontemplated herein that in other embodiments of an infusion device (notshown), each medication delivery channel and the associated one of thecannulas 514 do not have an essentially straight longitudinal axis.

Each one of the self-sealing members 516 is mounted within a respectivemedication delivery channel 526 with an exposed surface of each one ofthe self-sealing members 516 being essentially contiguous with theaccessible surface 518 of the body 512. Each one of the self-sealingmembers 516 forms a septum extending across the respective medicationdelivery channel 526. Each septum limits contaminants entering themedication delivery channel 526 and limits the back-flow of medicationfrom the medication delivery channel 526 through the respective one ofthe single inlet ports 20.

The adhesive laminate member 517 is mounted on the engagement surface522 of the body 512. The adhesive laminate member 517 includes anadhesive layer disposed between a substrate layer and a release linerlayer. The substrate layer provides structural integrity for theadhesive layer and is attached to the body 512. The release liner isremovable from the adhesive layer for engaging the adhesive layer to bebonded to a skin surface of the patient during mounting of the infusiondevice 500, thereby securing the infusion device 500 to a patient'sbody.

Each medication delivery channel 526 includes a tapered portion 530adjacent to the accessible surface 518 of the body 512. The taperedportion 530 of each medication delivery channel 526 forms afunnel-shaped entry into the respective medication delivery channel 526.The tapered portion 530 of each medication delivery channel 526 isintended to aid a patient in engaging an injection needle of a syringein a relatively quick and convenient manner by providing an insertionarea for the needle that is suitably larger than a cross sectional areaof the injection needle.

The tapered portion 530 of each medication delivery channel 526 istapered in a manner such that the respective one of the single inletports 520 has a minor diametrical dimension at least about two timesgreater than a minor diametrical dimension of the same medicationdelivery channel 526. A nominal diametrical dimension of an essentiallynon-tapered portion of the medication delivery channel (e.g., adjacentto the single outlet port 524) is an example of the minor diametricaldimension of the medication delivery channel 526. Examples of port andchannel cross-sectional profiles include round, rectangular, triangular,elliptical and other known profiles. In one embodiment of the singleinlet ports 520 and each medication delivery channel 526, each one ofthe single inlet ports 520 and each medication delivery channel 526 havea substantially circular cross-sectional profile and the single inletport 526 is essentially circular. In such an embodiment, the opening(i.e. a circular shaped opening) has a diameter at least about two timesgreater than a minor diameter of the medication delivery channel.

The body 512 further includes a plurality of identification features 536on the accessible surface 518. Each one of the identification features536 encompasses a respective one of the single inlet ports 520. Each oneof the identification features 536 is intended to aid in identifying therespective one of the single inlet ports 530. A first one of theidentification features 536 is raised with respect to the accessiblesurface 518 of the body 512 and a second one of the identificationfeatures 536 is recessed with respect to the accessible surface 518 ofthe body 512.

It is contemplated herein that identification features in accordancewith embodiments of the disclosures made herein may be at leastpartially raised with respect to an accessible surface of a respectivebody, may be at least partially recessed with respect to an accessiblesurface of a respective body or a combination of both raised andrecessed with respect to an accessible surface of a respective body. Itis also contemplated herein that identification features in accordancewith embodiments of the disclosures made herein may be a different colorthan a respective body and/or self-sealing material. It is yet furthercontemplated herein that identification features in accordance withembodiments of the disclosures made herein may be any one of a pluralityof shapes (e.g., round, rectangular, triangular, elliptical, etc.).

FIG. 8 depicts an infusion device 600 in accordance with a seventhembodiment of the disclosures made herein. The infusion device 600 issimilar in structure to the infusion device 500 depicted in FIG. 7. Theinfusion device 500 depicted in FIG. 7 and the infusion device 600depicted in FIG. 8 are both multi-cannula infusion devices. Structuralelements and features of the infusion device 600 and the infusion device10 (depicted in FIGS. 1 and 2) are similarly denoted. For example, thebody of the infusion device 600 is denoted as 612, whereas the body ofthe infusion device 500 is denoted as 512. Such similar elements andfeatures are denoted in FIG. 8, but may not be discussed in specificdetail in reference to FIG. 8.

The infusion device 600 includes a body 612 and a self-sealing member616 mounted on an accessible surface 618 of the body 612. The bodyincludes a plurality of inlet ports 620, a plurality of outlet ports 624and a plurality of discrete medication delivery channels 626. Each oneof the discrete medication delivery channels is connected between arespective one of the inlet ports 620 and a respective one of the outletports 624. The self-sealing member 616 forms a septum extending across aplurality of the medication delivery channels 626. Although theself-sealing member 616 is depicted as covering only a portion of theaccessible surface 618 of the body 612, it is contemplated and disclosedherein that the self-sealing member 616 may cover essentially the entireaccessible surface 618 of the body 612. The self-sealing member 616includes a plurality of integral identification features 636. One orboth of the identification features 636 encompasses a respective one ofthe inlet ports 620. The identification feature 636 toward the left sideof FIG. 8 is depicted as being a polygon.

It is contemplated herein that structural elements and featuresdiscussed herein in reference to single cannula infusion devices ofFIGS. 1 through 6, but not specifically discussed in reference tomulti-cannula infusion devices, may be applied to multi-cannula infusiondevices in accordance with embodiments of the disclosures made herein.For example, a needle stop may be applied to a multi-cannula infusiondevice in accordance with an embodiment of the disclosures made herein.Similarly, a septum may be provides at each outlet port.

It is also contemplated herein that a first structural element orfeatures discussed herein in reference to a particular embodiment of asingle cannula infusion device may be implemented in combination with asecond structural element or feature discussed herein in reference toanother particular embodiment of a single cannula infusion device, eventhough such combination is not specifically shown. One example wouldinclude implementing a needle stop in combination with a self-sealingmember that is mounted on the accessible surface of a body. Anotherexample would include implementing a self-sealing member mounted on theaccessible surface of a body in combination with a self-sealing memberthat is mounted adjacent to an engagement surface of the body.

Infusion devices in accordance with embodiments of the disclosures madeherein are capable of being fabricated using known techniques forforming elements of such infusion devices and for assembling suchelements. Injection molding, extrusion, thermal forming and the like areexamples of known techniques for forming such elements. Heat staking,ultrasonic welding, laser welding, solvent bonding and the like areexamples of known techniques for assembling such components.

Infusion devices in accordance with embodiments of the disclosures madeherein are capable of being fabricated from commercially availablematerials. Various polymers approved for use in medication applicationsby the United States Food and Drug Administration (U.S.F.D.A) areexamples of commercially available material from which elements ofinfusion devices may be made. For example, a material approved by theU.S.F.D.A. for use in invasive medical application is an example of amaterial from which cannula may be made. Materials approved by theU.S.F.D.A. for being exposed to therapeutic substances, but not approvedfor use in invasive applications, are examples of materials from whichthe body and septum may be made. In cases where the body and/or a septumof the infusion device are subjected to invasive conditions, a materialapproved by the U.S.F.D.A. for use in invasive medical application isappropriate.

It will be appreciated that infusion devices in accordance withembodiments of the disclosures made herein provide a reliable, safe,easy, fast, convenient and painless approach to delivering medicationssuch as insulin. Overall training and equipment costs are greatlyreduced through the use of such infusion devices. Additionally, suchinfusion devices provide great psychological benefits for patients,resulting from eliminating discomfort and mental distress oftenassociated with direct injections with a syringe. Generally speaking,such infusion devices will contribute to enhancing the overall qualityof life of many patients that require daily injections of medication.

Single cannula and multi-cannula infusion devices in accordance withembodiments of the disclosures made herein are subcutaneous infusionsites capable of being self-mounted by a patient. In one embodiment ofmounting such a single cannula or multi-cannula infusion device, aninsertion device capable of inserting the cannula into the subcutaneoustissue of the patient under a force applied by a spring, by air or thelike may be used. Various embodiments of insertion devices are known. Itwill be appreciated by a person of ordinary skill in the art that suchknown insertion devices may require certain modification for use withinfusion devices in accordance with embodiments of the disclosures madeherein.

Single cannula and multi-cannula infusion devices in accordance withembodiments of the disclosures made herein are intended to be worn andare capable of being worn for multiple days. Such infusion devicespermit daily direct injections with a syringe into the subcutaneoustissue of the patient, thereby precluding daily pain and discomfortassociated with injection needles. In this manner, the benefits ofdelivering a medication with a direct injection are provided, butwithout the drawbacks (e.g., multiple daily piercing of the skin). Withan infusion device in accordance to an embodiment of the disclosuresmade herein, the skin need only be pierced about every three days ormore for facilitating the associated direct inject.

A single cannula infusion device in accordance with an embodiment of thedisclosures made herein is particularly well-suited for enabling apatient to receive a single type of medication (e.g., insulin). However,if the patient is required to inject multiple types of medication thatare not compatible with each other (e.g., a bolus-type insulin and aBasal-type insulin), it is contemplated and disclosed herein that thepatient may use sterile saline solution to flush the single cannulainfusion device between injections of different medications.

Multi-cannula infusion devices represent another option for facilitatingthe delivery of multiple medications. A first medication can bedelivered via a first cannula and a second medication can be deliveredvia a second cannula. Similarly, by distributing a pluralityofinjections of a particular medication between a plurality of singlecannula infusion devices, the length of time that each of the pluralityof single cannula infusion devices may be worn is extended.

It is also contemplated that a multi-cannula infusion device inaccordance with an embodiment of the disclosures made herein or aplurality of single cannula devices may be used for extending the lengthof time that the infusion device may be worn. Tissue damage associatedwith pressure of delivering a medication and with the concentration ofthe medication are limiting factors in how long an infusion device maybe worn and/or used. Accordingly, by distributing a plurality ofinjections of a particular medication between a plurality of cannulas,the length of time that the infusion device may be worn is extended.

An embodiment of a method for distributing a plurality of medicationinjections using a multi-cannula infusion device as disclosed hereinincludes mounting a multi-cannula infusion device on a patient. Anembodiment of mounting the multi-cannula infusion device includesinserting each one of the cannulas into subcutaneous tissue of thepatient until an engagement surface of a body of the infusion deviceengages a skin surface of the patient. The multi-cannula infusion deviceincludes a plurality of insertion needles for facilitating its mounting.Each one of the insertion needles extends through a channel of arespective one of the cannulas for retaining the respective one of thecannulas in a generally straight orientation during insertion.

After mounting the multi-cannula infusion device on the patient andremoving the plurality of insertion needles, a first portion of aplurality of medication injections are administered to the patient via afirst medication delivery channel of the multi-cannula infusion deviceand a second portion of the plurality of medication injections to thepatient via a second medication delivery channel of the multi-cannulainfusion device. A length of the first one of the cannulas is greaterthan a length of the second one of the cannulas, thereby enabling thefirst portion of the plurality of medication injections to be deliveredat a first distance below a skin surface of the patient and enabling thesecond portion of the plurality of medication injections to be deliveredat a second distance below the skin surface of the patient.

An embodiment of a method for distributing a plurality of medicationinjections using a plurality of single cannula infusion devices asdisclosed herein includes mounting a plurality of single cannulainfusion devices on a patient. An embodiment of mounting each one of thesingle cannula infusion devices includes inserting the cannula of eachone of the single cannula infusion devices into subcutaneous tissue ofthe patient until an engagement surface of a body of each single cannulainfusion device engages a skin surface of the patient. Each one of thesingle cannula infusion device includes an insertion needles forfacilitating its mounting. Each one of the insertion needles extendsthrough a channel of a respective one of the cannulas for retaining therespective one of the cannulas in a generally straight orientationduring insertion.

In one embodiment of mounting the plurality of infusion devices, a firstone of the infusion devices is mounted at a first location on thepatient and a second one of the infusion devices is mounted at a secondlocation on the patient. A first physiological portion of the patientsuch as a first leg is an example of the first location. A secondphysiological portion of the patient such as a left hip is an example ofthe second location.

After mounting the plurality of single cannula infusion devices on thepatient and removing the insertion needles from each of the infusiondevices, a first portion of a plurality of medication injections areadministered to the patient via a first cannula of the multi-cannulainfusion device and a second portion of the plurality of medicationinjections to the patient via a second cannula of the multi-cannulainfusion device. A length of the cannula of the first infusion device isgreater than a length of the cannula of the second infusion device,thereby enabling the first portion of the plurality of medicationinjections to be delivered at a first distance below a skin surface ofthe patient and enabling the second portion of the plurality ofmedication injections to be delivered at a second distance below theskin surface of the patient.

In the preceding detailed description, reference has been made to theaccompanying drawings that form a part hereof, and in which are shown byway of illustration specific embodiments in which the invention may bepracticed. These embodiments, and certain variants thereof, have beendescribed in sufficient detail to enable those skilled in the art topractice the invention. To avoid unnecessary detail, the descriptionomits certain information known to those skilled in the art. Forexample, certain dimensions of elements of an infusion device, certainorientations of elements, specific selection of materials for variouselements and the like may be implemented based on an engineeringpreference and/or a specific application requirement. The precedingdetailed description is, therefore, not intended to be limited to thespecific forms set forth herein, but on the contrary, it is intended tocover such alternatives, modifications, and equivalents, as can bereasonably included within the spirit and scope of the appended claims.

1. An infusion device comprising: a body having a body passageway; acannula having a portion extending from the body, the cannula alsohaving a cannula passageway defined by a cannula passageway wall, thecannula passageway wall having an inwardly-tapered portion that will beabove a patient's skin when the infusion device is used, the cannulapassageway having a cannula passageway end positioned outside the body,the cannula passageway end having a width, a septum positioned withinthe body passageway, the septum having a septum top surface thatincludes a septum top surface portion accessible to an injection needle,the septum top surface portion having a septum cross-section positionedperpendicular to an axis that is centered in the body passageway, theseptum cross-section having a greatest width that is greater than thewidth of the cannula passageway end; and an inner surface that directlyborders open space within the body passageway that is downstream of theseptum and upstream of the inwardly-tapered cannula passageway wallportion, the inner surface defining a first inner surface perimeterpositioned in a first plane that is perpendicular to the axis, the innersurface also defining a second inner surface perimeter positioned in asecond plane that is parallel to and downstream of the first plane, thefirst inner surface perimeter defining a first cross-sectional area, thesecond inner surface perimeter defining a second cross-sectional area,and the first cross-sectional area being greater than the secondcross-sectional area; the infusion device being configured such that (a)a first portion of the infusion device is above the patient's skinsurface when the infusion device is used and (b) a second portion of theinfusion device is beneath the patient's skin surface when the device isused, the first portion having a first portion height measured along theaxis, the second portion having a second portion height measured alongthe axis, the second portion height being greater than the fist portionheight.
 2. The infusion device of claim 1, in which the septum includesan outer wall extending from the septum top surface that includes aninwardly-tapered portion.
 3. The infusion device of claim 1, in whichthe body includes a top and a bottom, the septum includes a bottom, andthe infusion device includes (a) a first greatest distance parallel tothe axis between the septum top surface and the top of the body and (b)a second greatest distance parallel to the axis between the bottom ofthe septum and the bottom of the body, the second greatest distancebeing greater than the first greatest distance.
 4. The infusion deviceof claim 1, in which the body includes an inlet to the body passagewayand an identification feature adjacent to the inlet for identifying thebody passageway.